上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Cytochalasin K
Cytochalasin K (Compounds 7) 是一种抑制小麦根系伸长的细胞松弛素,IC50 为 22.58 μM。
Cytochalasin K Chemical Structure
CAS No. : 79648-72-9
规格
是否有货
100 mg
询价
250 mg
询价
500 mg
询价
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生物活性
Cytochalasin K (Compounds 7) is a cytochalasin that inhibits wheat root elongation with an IC50 of 22.58 μM[1].
分子量
531.64
Formula
C32H37NO6
CAS 号
79648-72-9
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Wen-Bo Han, et al. Cytochalasins and an Abietane-Type Diterpenoid with Allelopathic Activities from the Endophytic Fungus Xylaria Species. J Agric Food Chem. 2019 Apr 3;67(13):3643-3650.
Oleonuezhenide, isolated from Fructus Ligustri Lucidi, exerts neuroprotective effects[1].
分子量
1073.01
Formula
C48H64O27
CAS 号
112693-21-7
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moisture and light
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
参考文献
[1]. Deng X, et al. The combined effect of oleonuezhenide and wedelolactone on proliferation and osteoblastogenesis of bone marrow mesenchymal stem cells. Phytomedicine. 2019 Dec;65:153103.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Valeriandoid F
Valeriandoid F 是一种环烯醚萜,可有效抑制 NO 的产生,IC50 值为 0.88 μM。Valeriandoid F 具有抗炎和抗增殖活性。
Valeriandoid F Chemical Structure
CAS No. : 1427162-60-4
规格
是否有货
5 mg
询价
10 mg
询价
25 mg
询价
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生物活性
Valeriandoid F is an iridoid, which potently inhibits NO production with an IC50 value of 0.88 μM. Valeriandoid F has anti-inflammatory and antiproliferative activities[1].
体外研究 (In Vitro)
Valeriandoid F selectively inhibits the proliferation of human glioma stem cell lines, GSC-3 and GSC-18, with IC50 values of 7.16 μM and 5.75 μM, respectively[1].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
454.51
Formula
C23H34O9
CAS 号
1427162-60-4
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Huan Liu, et al. Iridoids from Valeriana jatamansi with anti-inflammatory and antiproliferative properties. Phytochemistry. 2021 Apr;184:112681.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Hederasaponin B(Synonyms: 刺五加叶中)
Hederasaponin B 是从 Hedera helix 中分离的,具有针对肠道病毒 71 (EV71) 各种亚型的广谱抗病毒活性。
Hederasaponin B Chemical Structure
CAS No. : 36284-77-2
规格
价格
是否有货
数量
5 mg
¥2350
In-stock
10 mg
¥4000
In-stock
50 mg
询价
100 mg
询价
* Please select Quantity before adding items.
Hederasaponin B 相关产品
•相关化合物库:
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生物活性
Hederasaponin B, isolated from Hedera helix, has broad-spectrum antiviral activity against various subgenotypes of Enterovirus 71 (EV71).
分子量
1205.38
Formula
C59H96O25
CAS 号
36284-77-2
中文名称
刺五加叶中
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moisture and light
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
参考文献
[1]. Song J, et al. Antiviral Activity of Hederasaponin B from Hedera helix against Enterovirus 71 Subgenotypes C3 and C4a. Biomol Ther (Seoul). 2014 Jan;22(1):41-6.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Lindenenol(Synonyms: 乌药醇)
Lindenenol 可从Radix linderae 中分离得到,具有抗氧化和抗菌活性。
Lindenenol Chemical Structure
CAS No. : 26146-27-0
规格
价格
是否有货
数量
5 mg
¥3360
In-stock
10 mg
¥5710
In-stock
50 mg
询价
100 mg
询价
* Please select Quantity before adding items.
Lindenenol 相关产品
•相关化合物库:
Natural Product Library Plus
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Natural Product Library
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Terpenoids Library
Traditional Chinese Medicine Monomer Library
生物活性
Lindenenol is isolated from Radix linderae, with antioxidant and antibacterial activities[1].
分子量
230.30
Formula
C15H18O2
CAS 号
26146-27-0
中文名称
乌药醇
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moisture and light
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
参考文献
[1]. Joshi SC, et al. Antioxidant and antibacterial activities of the leaf essential oil and its constituents furanodienone and curzerenone from Lindera pulcherrima (Nees.) Benth. ex hook. f. Pharmacognosy Res. 2012 Apr;4(2):80-4.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Eupalinolide B(Synonyms: 野马追内酯B) 纯度: 99.28%
Eupalinolide B 是从 Eupatorium lindleyanum 分离的胚芽倍半萜。 Eupalinolide B 对 A-549,BGC-823 和 HL-60 等肿瘤细胞具有细胞毒性。
Eupalinolide B Chemical Structure
CAS No. : 877822-41-8
规格
价格
是否有货
数量
5 mg
¥3360
In-stock
10 mg
¥5710
In-stock
50 mg
询价
100 mg
询价
* Please select Quantity before adding items.
Eupalinolide B 相关产品
•相关化合物库:
Covalent Screening Library Plus
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生物活性
Eupalinolide B is a germacrane sesquiterpene isolated from Eupatorium lindleyanum. Eupalinolide B demonstrates potent cytotoxicity against A-549, BGC-823 and HL-60 tumour cell lines[1].
分子量
462.49
Formula
C24H30O9
CAS 号
877822-41-8
中文名称
野马追内酯B
运输条件
Room temperature in continental US; may vary elsewhere.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Chlorahololide C
Chlorahololide C 是一种从 Chloranthus holostegius 中分离得到林丹倍半萜类二聚体。Chlorahololide C 是一种有效和选择性的钾通道阻滞剂,IC50 值为 3.6 μM。
Chlorahololide C Chemical Structure
CAS No. : 1007859-25-7
规格
是否有货
5 mg
询价
10 mg
询价
25 mg
询价
* Please select Quantity before adding items.
生物活性
Chlorahololide C, a lindenane sesquiterpenoid dimer, is isolated from Chloranthus holostegius. Chlorahololide C is a potent and selective potassium channel blocker, with an IC50 of 3.6 μM[1].
IC50 & Target
IC50: 3.6 μM (potassium channel)[1]
体外研究 (In Vitro)
Chlorahololide C (0.1-100 μM) inhibits the delayed rectifier K+ current (IK) in rat dissociated hippocampal neurons, with an IC50 of 3.6 μM[1].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
576.63
Formula
C33H36O9
CAS 号
1007859-25-7
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Yang SP, et, al. Chlorahololides C-F: a new class of potent and selective potassium channel blockers from Chloranthus holostegius. Tetrahedron. 2008 Feb; 64(9):2027-2034.
Polygodial (Poligodial) is an antifungal potentiator[1]. Polygodial is a sesquiterpene with anti-hyperalgesic properties[2].
体外研究 (In Vitro)
Polygodial exhibits fungicidal activity against Saccharomyces cerevisiae, Candida albicans, and other fungal pathogens in standardized susceptibility tests (NCCLS). Polygodial (12.5 μg/mL, 3 hours) induces significant shrinkage compared to controls in Saccharomyces cerevisiae cells with the minimum fungicidal concentration (MFC) for 106 CFU/mL in RPMI 1640 medium[3].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Viability Assay[3]
Cell Line:
S. cerevisiae cells
Concentration:
12.5 μg/mL
Incubation Time:
3 hours
Result:
Treated cells exhibited significant shrinkage compared to controls, and the organization of subcellular organelles appears either disrupted or compacted.
体内研究 (In Vivo)
Polygodial is a sesquiterpene isolated from the barks of Drymis winteri (Winteraceae). Polygodial (0.5 to 10 mg/kg; 0.5 h; given by i.p. route to mice) induces significant, dose-related and almost complete inhibition of Acetic acid, Kaolin and Zymosan-induced abdominal constrictions. The calculated mean ID50 values are 0.8, 2.1 and 2.6 mg/kg and maximal inhibitions of 90.0±3.0, 98.0±1.0 and 97.0±2.0 %, against Acetic acid, Kaolin and Zymosan, respectively. Polygodial is about 14- to 27-fold more potent than the hydroalcoholic extract (HE) at the ID50 level[2].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
Non-fasted male Swiss mice (20-30 g) or male Wistar rats (150-180 g)[2]
Dosage:
0.1 to 10 mg/kg
Administration:
Injected i.p. 0.5 h before the injection of irritant substances
Result:
Produced significant inhibition of Acetic acid, Kaolin and Zymosan-induced writhing in mice.
分子量
234.33
Formula
C15H22O2
CAS 号
6754-20-7
中文名称
蓼二醛
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. I Kubo, et al. Polygodial, an antifungal potentiator. J Nat Prod. Jan-Feb 1988;51(1):22-9.
[2]. G L Mendes, et al. Anti-hyperalgesic properties of the extract and of the main sesquiterpene polygodial isolated from the barks of Drymis winteri (Winteraceae). Life Sci. 1998;63(5):369-81.
[3]. C S Lunde, et al. Effect of polygodial on the mitochondrial ATPase of Saccharomyces cerevisiae. Antimicrob Agents Chemother. 2000 Jul;44(7):1943-53.